REPORTING INTEGRATOR 3392A— 510(k) K833113
Substantially EquivalentHewlett-Packard Co.
FDA 510(k) clearance K833113 for REPORTING INTEGRATOR 3392A, Substantially Equivalent on 1983-11-21. Applicant: Hewlett-Packard Co.. Device class: 1.
Clearance details
- Applicant
- Hewlett-Packard Co.
- Product code
- Code LDM
- Device class
- Class 1
- Regulation
- 21 CFR 862.2260
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Recent devices under product code LDM
view allMore clearances from Hewlett-Packard Co.
view all- K992543 — HEARTSTREAM XLT DEFIBRILLATOR/MONITOR, AC CHARGER, DC CHARGER, DATA CARD, SINGLE BAY ADAPTER, DEFIBRILLATOR PADS CABLE
- K993587 — HP M2376A DEVICE LINK SYSTEM
- K993169 — MODIFICATION OF: PHYSIOLOGICAL SIGNAL TRANSMITTER AND RECEIVER, MODEL 3810A
- K992977 — HEWLETT PACKARD MULTIFUNCTION PEDIATRIC DEFIB FUNCTION, MODEL M3503A & M3504A
- K993516 — HP M2600A VIRIDIA TELEMETRY SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.